RGD:405236330 Rat Genome Database

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Variant: RGD:405236330 -  Homo sapiens

RGD ID: 405236330
ClinVar ID: CV3038082
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: USP7  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 8,993,578
GRCh38 16 8,899,721
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001286458.2:c.2049C>T
NM_001321858.2:c.2172C>T
NM_001286457.2:c.2298C>T
NM_003470.3:c.2346C>T
More... 		12/16/2022 non-coding transcript variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003712420 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene USP7 CLINVAR
OMIM 602519 CLINVAR